Disuccinimidyl glutarate, 97%, Thermo Scientific Chemicals
Disuccinimidyl glutarate, 97%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Disuccinimidyl glutarate, 97%, Thermo Scientific Chemicals

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Quantity:
500 mg
100 mg
Catalog number H58208.ME
also known as H58208-ME
Price (USD)/ Each
423.65
Online exclusive
470.00 
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Quantity:
500 mg
Request bulk or custom format
Price (USD)/ Each
423.65
Online exclusive
470.00 
Save 46.35 (10%)
Add to cart
Disuccinimidyl glutarate, 97%, Thermo Scientific Chemicals
Catalog numberH58208.ME
Price (USD)/ Each
423.65
Online exclusive
470.00 
Save 46.35 (10%)
-
Add to cart
Chemical Identifiers
CAS79642-50-5
IUPAC Namebis(2,5-dioxopyrrolidin-1-yl) pentanedioate
Molecular FormulaC13H14N2O8
InChI KeyLNQHREYHFRFJAU-UHFFFAOYSA-N
SMILESO=C(CCCC(=O)ON1C(=O)CCC1=O)ON1C(=O)CCC1=O
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White to cream
FormCrystals or crystalline powder or powder
Assay from Suppliers CofA≥96.0% (TLC)
Identification (FTIR)Conforms
Melting Point130-136°C
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Disuccinimidyl glutarate is used as a membrane-soluble, amine-reactive N-hydroxysuccinamide ester-based homobifunctional crosslinking reagent. It is a homobifunctionla cross-linking reagent, for ex. isolation of the insulin receptor.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Disuccinimidyl glutarate is used as a membrane-soluble, amine-reactive N-hydroxysuccinamide ester-based homobifunctional crosslinking reagent. It is a homobifunctionla cross-linking reagent, for ex. isolation of the insulin receptor.

Solubility
Soluble in dimethylsulfoxide and dimethylformamide. Partially soluble in water.

Notes
Moisture sensitive. Store in a cool place. Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Morioka, T.; Loik, N. D.; Hipolito, C. J.; Goto, Y.; Suga, H. Selection-based discovery of macrocyclic peptides for the next generation therapeutics. Curr. Opin. Chem. Biol. 2015, 26, 34-41.
  2. Smaldone, G.; Diana, D.; Pollegioni, L.; Di Gaetano, S.; Fattorusso, R.; Pedone, E. Insight into conformational modification of alpha-synuclein in the presence of neuronal whole cells and of their isolated membranes. FEBS Lett. 2015, 589 (7), 798-804.